SYNTHESIS PORTFOLIO (PART I) Synthesis of 1 2-epoxycyclopentane I. MATERIALS CAS # or Catalogue # from a supplier Chemicals / Reagents (Example: Sigma Aldrich) Apparatus / Equipment: (Indicate below) II. EXPERIMENTAL PROCEDURE II. DISCUSSION (Explain the Chemistry behind the synthesis process.)
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- Provide the conditions and show the curved arrow mechanism and Intermediate for the reactions leading to 1 or 2 selectivelyMatch the reagents, materials and parameters to its appropriate description.Write out the reaction of Bromination of E-stilbene using chemdraw (ACS 1996 format). Include all reagents, products, solvents, reaction temperature and yield. Reagents used include glacial acetic acid, E-stilbene, and pyridinium perbromide, otherwise known as PHPB. Glacial acetic acid: 10mL Stilbene: 0.5g Perbromide: 1.0g Product yield (Precipitate) weight: 0.63g
- I need specific description of the compounds involved in the synthesis (functional groups, specific features). and also describe the steps involved in the synthesis and the role of each step. And most important!!devote one to each step of the synthesis. Each step should clearly indicate the reagent used, the stereochemistry involved in the reaction and its importance or relevance to the multistep synthesisPlease provide detailed mechanism for this reaction.What is the role of Amberlyst I-120 plus resin? Thanks so much.A full arrow pushung mechanism for the reactions and show their intermediates
- can you explain your drawings in the reaction scheme and on the answers too?What does In-situ mean in the case of In-situ reaction? example down below Benzyne is a highly reactive organic molecule that has not been isolated. It is prepared in situ reaction. Its instability is the result of its triple bond.Describe every aspect of the procedure clearly and explicitly. Include temperatures, appearance of the reaction (include pictures!). How is the reaction monitored? Is the order of addition important? 4,4'-DIBROMOBIPHENYL [Biphenyl, 4,4'-dibromo-] Submitted by Robert E. Buckles and Norris G. Wheeler1. Checked by R. S. Schreiber, Wm. Bradley Reid, Jr., and Robert W. Jackson. 1. Procedure In a 15-cm. evaporating dish is placed 15.4 g. (0.10 mole) of finely powdered biphenyl (Note 1). The dish is set on a porcelain rack in a 30-cm. desiccator with a 10-cm. evaporating dish under the rack containing 39 g. (12 ml., 0.24 mole) of bromine. The desiccator is closed, but a very small opening is provided for the escape of hydrogen bromide (Note 2). The biphenyl is left in contact with the bromine vapor for 8 hours (or overnight). The orange solid is then removed from the desiccator and allowed to stand in the air under a hood for at least 4 hours (Note 3). At this point, the product weighs…
- Fast pls in 5 min will give u like for sure Create a synthesis of the heterocyclic compound 5 from starting materials each containing no more than six carbon atoms.In the solution you should use retrosynthetic analysis to justify your choice.(Give clear handwritten solution) give reaction mechanism and major product for the all three subparts (a,b and c) solution.Give reaction mechanism in clear handwritten on paper!